Last Updated: September 28, 2026

Details for New Drug Application (NDA): 022244

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NDA 022244 describes LUSEDRA, which is a drug marketed by Eisai Inc and is included in one NDA. Additional details are available on the LUSEDRA profile page.

The generic ingredient in LUSEDRA is fospropofol disodium. There is one drug master file entry for this compound. Additional details are available on the fospropofol disodium profile page.

Summary for 022244

Tradename:	LUSEDRA
Applicant:	Eisai Inc
Ingredient:	fospropofol disodium
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION;INTRAVENOUS			Strength	1050MG/30ML (35MG/ML)
Approval Date:	Dec 12, 2008	TE:		RLD:	No

Expired US Patents for NDA 022244

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Eisai Inc	LUSEDRA	fospropofol disodium	SOLUTION;INTRAVENOUS	022244-001	Dec 12, 2008	⤷ Start Trial	⤷ Start Trial
Eisai Inc	LUSEDRA	fospropofol disodium	SOLUTION;INTRAVENOUS	022244-001	Dec 12, 2008	⤷ Start Trial	⤷ Start Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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